美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
46122-801-08	46122-801	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20241001	N/A	ANDA	ANDA213203	Amerisource Bergen	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (46122-801-08) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
79481-1002-1	79481-1002	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20210715	N/A	ANDA	ANDA213203	Meijer	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (79481-1002-1) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
58602-834-77	58602-834	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20200325	N/A	ANDA	ANDA213203	Aurohealth LLC	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	1200 mg/1; 120 mg/1	1 BLISTER PACK in 1 CARTON (58602-834-77) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
58602-834-78	58602-834	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20200325	N/A	ANDA	ANDA213203	Aurohealth LLC	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	1200 mg/1; 120 mg/1	2 BLISTER PACK in 1 CARTON (58602-834-78) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0363-0134-78	0363-0134	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20200805	N/A	ANDA	ANDA213203	WALGREEN CO.	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	1200 mg/1; 120 mg/1	2 BLISTER PACK in 1 CARTON (0363-0134-78) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0363-9946-40	0363-9946	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20220507	N/A	ANDA	ANDA213203	WALGREEN CO.	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (0363-9946-40) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0363-9946-45	0363-9946	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20220507	N/A	ANDA	ANDA213203	WALGREEN CO.	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	2 BLISTER PACK in 1 CARTON (0363-9946-45) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
58602-833-12	58602-833	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20200325	N/A	ANDA	ANDA213203	Aurohealth LLC	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (58602-833-12) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
58602-833-17	58602-833	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20200325	N/A	ANDA	ANDA213203	Aurohealth LLC	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	2 BLISTER PACK in 1 CARTON (58602-833-17) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
30142-137-12	30142-137	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20210416	N/A	ANDA	ANDA213203	KROGER COMPANY	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (30142-137-12) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
30142-137-17	30142-137	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCl	TABLET, EXTENDED RELEASE	ORAL	20210416	N/A	ANDA	ANDA213203	KROGER COMPANY	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	2 BLISTER PACK in 1 CARTON (30142-137-17) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK